Canonical Allele Identifier: PA2829392534
Gene: RAD51C HGNC NCBI

Linked Data

ClinVar Variation Id: 182834
ClinVar RCV Id: RCV000160922 RCV000206110 RCV000218584 RCV001798558 RCV003467268
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002867.1:p.Thr132Arg
CA299882
NM_002876.4:c.395C>G